Canonical Allele Identifier: CA788486252

Gene:

Linked Data

• dbSNP Id: rs1291344084
• MyVariant Identifiers: chr4:g.145480442C>A (hg19) ; chr4:g.144559290C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144559290C>A , CM000666.2:g.144559290C>A	GRCh38
NC_000004.11:g.145480442C>A , CM000666.1:g.145480442C>A	GRCh37
NC_000004.10:g.145699892C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649263.1:c.328-143312G>T	ENSP00000497507.1:n.328-143312G>T
XR_939272.1:n.178+2694G>T
XR_939273.1:n.178+2694G>T
XR_939272.2:n.522+2694G>T
XR_939273.2:n.522+2694G>T